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Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionAt Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in...
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Medical Science Liaison/Senior MSL
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Senior Director, US Medical Affairs Solid Tumor Portfolio NJ: Lead the Charge in Cancer Treatment
2 months ago
Genmab is seeking a highly skilled and experienced Senior Director to lead our US Medical Affairs team for the Solid Tumor Portfolio. As a key member of our leadership team, you will be responsible for building and leading a high-performing team, developing and executing strategic plans, and providing US market perspective to the development of our solid tumor assets.
Key Responsibilities- Build, lead, and oversee the productivity of the US in-house Medical Affairs solid tumor team, attracting and developing strong talent for Genmab.
- Establish a supportive and thriving culture for USMA, contributing to the development of a high-performing leadership team.
- Lead the development of the USMA strategic plans for the solid tumor portfolio/assets and oversee the execution of tactics, working in close collaboration with cross-functional matrix colleagues.
- Accountable for ensuring USMA launch readiness (for solid tumor assets/indications) and supports cross-functional launch activities.
- Serve as a medical and content expert for internal and external stakeholders, representing Genmab at key global and US medical conferences, at US advisory boards, and at internal training forums.
- Develop and maintain positive professional relationships with US thought-leaders based on mutual respect and reciprocal scientific information exchange related to medical therapies.
- Provide US market input to global clinical development and global medical affairs programs, staying abreast of the evolving scientific and competitive landscape for relevant solid tumors.
- Serve as the USMA lead on solid tumor lifecycle strategy, including evidence generation strategy development and execution of Phase 3b/4 medical affairs-led interventional and observational clinical trials.
- Ensure US market needs are satisfied within integrated evidence generation plans and ensure development and updates of areas of interest reflective of US needs.
- Provide scientific input and strategic direction to the investigator-sponsored trial program for solid tumor assets/disease and participate in the review of all US ISTs.
- Ensure the delivery of timely, accurate, and succinct communication of fair-balanced clinical and scientific presentations to healthcare professionals, both proactively and in response to requests for information, consistent with promotional compliance and regulatory requirements.
- Develop and maintain a network of cooperative groups, medical societies, and patient advocacy groups to enable insights to local unmet medical research needs and educational gaps.
- Coach, oversee, and conduct performance evaluations of medical affairs personnel via active observation of the team, establishment of clearly defined team and individual goals and objectives (quantitative and qualitative), and implementation of processes to routinely monitor progress.
- Collaborate effectively and in a compliant manner with colleagues in other functional areas.
- Ensure optimal safety, clinical oversight, and highest quality standards are applied to all US medical affairs solid tumor portfolio-related work.
- Responsible for ensuring compliance and accountable for local adherence to company procedures and local regulations.
- Advanced scientific background (MD, PharmD, DPN, Ph.D.); oncology experience required; gyn/onc preferred.
- Minimum of 10 years of experience in a senior leadership role within the pharmaceutical or biotechnology industry.
- Deep knowledge of drug development and a strong track record of success in the field.
- Proven ability to develop and execute medical and scientific strategies that drive business results and successful commercialization of new drug entities and assets.
- Excellent leadership and team management skills, with experience building and leading high-performing teams.
- Excellent communication and interpersonal skills, capable of effectively engaging with diverse stakeholders.
- Ability to adapt to rapidly changing market conditions and technological advancements.
- Strong analytical and problem-solving skills, with a data-driven approach to decision-making.
- Regulatory experience is a plus.
- Willingness to travel 25-30% of the time, both globally and domestically.
